Canonical Allele Identifier: PA2580265290
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2247345
ClinVar RCV Id: RCV002781743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Val3539Phe
CA1103258
NM_002016.2:c.10615G>T